Glycerol oxidation-assisted electrochemical CO2 reduction for the dual production of formate

被引:49
作者
Pei, Yuhou [1 ]
Pi, Zhenfeng [1 ]
Zhong, Heng [1 ,2 ]
Cheng, Jiong [1 ]
Jin, Fangming [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Sch Environm Sci & Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Ctr Hydrogen Sci, Shanghai, Peoples R China
[3] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
基金
国家重点研发计划; 上海市自然科学基金; 中国国家自然科学基金;
关键词
LAYERED DOUBLE HYDROXIDES; BIFUNCTIONAL ELECTROCATALYST; CARBON NITRIDE; FORMIC-ACID; EFFICIENT; GRAPHENE; NICKEL; PERFORMANCE; COBALT; NI;
D O I
10.1039/d1ta07119j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The sluggish oxygen evolution reaction (OER) is one of the main bottlenecks for efficient CO2 electroreduction (CO2ER). Seeking a suitable organic oxidation reaction with a lower redox potential to replace the OER is a promising method to boost the overall efficiency of the CO2ER. Here, we propose a method of substituting the OER with a glycerol oxidation reaction (GOR) for the CO2ER to achieve the coproduction of formate at both the cathode and anode. A two-electrode GOR-assisted CO2ER system is successfully established with a Ni foam-supported surface-sulfurized nickel-cobalt hydroxide nanoneedle catalytic anode (Ni0.33Co0.67(OH)(2)@HOS/NF) and a BiOI cathode. The simultaneous formation of formate from the anodic GOR and cathodic CO2ER with faradaic efficiencies (FEs) of 90% and 92%, respectively, is obtained at a cell voltage of 1.9 V (22.4 mA cm(-2)). More significantly, an overall electricity-to-formate energy conversion efficiency of 110% is obtained in our GOR-assisted CO2ER system. This work not only proposes an energy- and atom-efficient method for the CO2ER but also provides new insights for developing highly active non-noble metal catalysts for the GOR.
引用
收藏
页码:1309 / 1319
页数:12
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